Amantadine Capsules

Name: Amantadine Capsules
Brand: Artemisine Medicines Technology Co., Ltd.

Capsules

Amantadine Capsules — GMP manufactured capsules by Artemisine Medicines Technology. Original manufacturer supply with stable quality, factory direct price and full batch documentation for global markets.

Product Name	Amantadine Capsules
Dosage Form	Capsules
Strength	100 mg
Standards	BP / ENTERPRISE
Packing	Customized per market requirement (bottle / blister / box)
Documents	COA, COPP, DMF, CTD Dossiers
MOQ	Contact us for MOQ and current stock

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WHO Prescribing Guidance

Indications · Administration · Dosage · Precautions

Reference information summarised from WHO prescribing guidance. Expand each item below — clinical use must always follow the locally approved product insert.

🎯Indications▾

Influenza A treatment/prophylaxis (where circulating strains are susceptible) and symptomatic treatment of Parkinson's disease/drug-induced dyskinesia.

💧Administration▾

Oral capsules/syrup; renal function determines dosing interval. Start at the beginning of symptoms for influenza.

⚖️Dosage▾

Adults 100–200 mg daily; elderly 100 mg daily; children 1–9 years 5 mg/kg/day (max 150 mg/day). Reduce dose in renal impairment.

⚠️Precautions & Warnings▾

Common: insomnia, dizziness, anxiety, livedo reticularis and peripheral oedema. Avoid in epilepsy, severe renal impairment and pregnancy; reduce dose in the elderly because of accumulation and hallucinations.

Reference: WHO Model Formulary / WHO Model List of Essential Medicines. For professional reference only — clinical use must follow the locally approved product insert and national treatment guidelines.

Why Order From Us

Factory Direct. Fully Documented.

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GMP Quality

Full batch testing and quality traceability under standard GMP workshops.

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Fast Delivery

Sufficient stock on regular items, familiar with export logistics to 50+ countries.

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Registration Support

COA, DMF, dossier and legalization documents for your market registration.

FAQ

Amantadine Capsules — Frequently Asked Questions

Which documents are provided for Amantadine Capsules registration?

Every batch of Amantadine Capsules ships with a Certificate of Analysis (COA). For market registration we provide COPP, DMF and CTD-format dossiers, plus legalisation support where your authority requires it.

What is the MOQ and lead time for Amantadine Capsules?

MOQ and lead time for Amantadine Capsules depend on strength, packaging and destination market. Send us your target market and annual volume — our export team confirms current stock, MOQ and lead time within 24 hours.

Do you support OEM / private label?

Yes. We offer OEM packaging and private-label production for Amantadine Capsules, subject to the regulatory requirements of the destination market.

Which markets have you exported capsules products to?

We have supplied capsules products to 50+ countries across Africa, Southeast Asia, Latin America and the Middle East, with experience in ministry-of-health registration and international tenders.

How is the quality of Amantadine Capsules controlled?

Amantadine Capsules is produced in China-GMP workshops (site re-inspected and passed in 2026), released only after full QC testing against BP / enterprise standards, with retained samples kept for one year beyond the product's expiry date.

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